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Items: 1 to 20 of 149

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5980451copy number variation1nstd102humanLikely pathogenic GRCh37 chr14: 54,654,001-75,828,024 , GRCh38.p12 chr14: 54,187,283-75,361,321 ACTN1, ACYP1, 400 more genes
    nsv5939871copy number variation1nstd209human GRCh38 chr14: 67,662,845-67,663,615 , GRCh37.p13 chr14: 68,129,562-68,130,332 VTI1B
    nsv5510731copy number variation1nstd206human GRCh38 chr14: 67,662,881-67,663,616 , GRCh37.p13 chr14: 68,129,598-68,130,333 VTI1B
    nsv5380972copy number variation2nstd102humanUncertain significance GRCh37 chr14: 65,937,790-68,354,021 , GRCh38.p12 chr14: 65,471,072-67,887,304 RPL21P9, LOC100419668, 35 more genes
    nsv5357350translocation1nstd200human GRCh38 chr14: 67,663,616-67,663,616 , GRCh38 chr14: 67,662,881-67,662,881 , GRCh37.p13 chr14: 68,130,333-68,130,333 , GRCh37.p13 chr14: 68,129,598-68,129,598 VTI1B
    nsv5338100translocation1nstd200human GRCh37 chr14: 68,130,333-68,130,333 , GRCh37 chr14: 68,129,598-68,129,598 , GRCh38.p12 chr14: 67,663,616-67,663,616 , GRCh38.p12 chr14: 67,662,881-67,662,881 VTI1B
    nsv5321655translocation1nstd204human GRCh38.p13 chr14: 67,662,881-67,662,881 , GRCh38.p13 chr14: 67,663,616-67,663,616 , GRCh37.p13 chr14: 68,129,598-68,129,598 , GRCh37.p13 chr14: 68,130,333-68,130,333 VTI1B
    nsv5274942copy number variation1nstd204human GRCh38.p13 chr14: 67,662,398-67,664,047 , GRCh37.p13 chr14: 68,129,115-68,130,764 VTI1B
    nsv5269924copy number variation1nstd204human GRCh38.p13 chr14: 67,662,901-67,663,600 , GRCh37.p13 chr14: 68,129,618-68,130,317 VTI1B
    nsv5181000mobile element insertion1nstd203human GRCh38 chr14: 67,668,154-67,668,174 , GRCh37.p13 chr14: 68,134,871-68,134,891 VTI1B
    nsv5032025inversion1nstd200human GRCh38 chr14: 53,190,097-88,878,877 , GRCh37.p13 chr14: 53,656,815-89,345,221 , IFT43, 578 more genes
    nsv4675709copy number variation1nstd102humanUncertain significance GRCh37 chr14: 67,331,167-68,451,970 , GRCh38.p12 chr14: 66,864,449-67,985,253 RDH11, RN7SL369P, 25 more genes
    nsv4675260copy number variation1nstd102humanUncertain significance GRCh37 chr14: 68,037,409-68,278,365 , GRCh38.p12 chr14: 67,570,692-67,811,648 PLEKHH1, RDH11, 13 more genes
    nsv4670413copy number variation1nstd186human GRCh37 chr14: 68,129,562-68,130,333 , GRCh38.p12 chr14: 67,662,845-67,663,616 VTI1B
    nsv4627435copy number variation1nstd183human GRCh37 chr14: 68,140,879-68,191,122 , GRCh38.p12 chr14: 67,674,162-67,724,405 RDH12, RN7SL369P, 3 more genes
    nsv4626860copy number variation1nstd183human GRCh37 chr14: 68,129,562-68,130,333 , GRCh38.p12 chr14: 67,662,845-67,663,616 VTI1B
    nsv4529257copy number variation1nstd166human GRCh37.p13 chr14: 67,433,394-68,147,101 , GRCh38.p12 chr14: 66,966,677-67,680,384 , SF3B4P1, 19 more genes
    nsv4455214copy number variation1nstd102humanUncertain significance GRCh37 chr14: 68,130,744-68,275,342 , GRCh38.p12 chr14: 67,664,027-67,808,625 RN7SL213P, RPL21P9, 6 more genes
    nsv4436741copy number variation1nstd102humanUncertain significance GRCh37 chr14: 68,110,557-68,283,783 , GRCh38.p12 chr14: 67,643,840-67,817,066 RN7SL213P, RNA5SP386, 9 more genes
    nsv4416592copy number variation1nstd174human GRCh37 chr14: 68,129,444-68,130,347 , GRCh38.p12 chr14: 67,662,727-67,663,630 VTI1B
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